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    Reactive oxygen species–associated molecular signature predicts survival in patients with sepsis

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    Author
    Bime, Christian
    Zhou, Tong
    Wang, Ting
    Slepian, Marvin J.
    Garcia, Joe G. N.
    Hecker, Louise
    Affiliation
    Univ Arizona, Dept Med
    Univ Arizona, Dept Biomed Engn
    Issue Date
    2016-06
    Keywords
    microarray
    gene expression
    reactive oxygen species
    sepsis
    
    Metadata
    Show full item record
    Publisher
    UNIV CHICAGO PRESS
    Citation
    Reactive oxygen species–associated molecular signature predicts survival in patients with sepsis 2016, 6 (2):196 Pulmonary Circulation
    Journal
    Pulmonary Circulation
    Rights
    © 2016 by the Pulmonary Vascular Research Institute. All rights reserved.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Sepsis-related multiple organ dysfunction syndrome is a leading cause of death in intensive care units. There is overwhelming evidence that oxidative stress plays a significant role in the pathogenesis of sepsis-associated multiple organ failure; however, reactive oxygen species (ROS)-associated biomarkers and/or diagnostics that define mortality or predict survival in sepsis are lacking. Lung or peripheral blood gene expression analysis has gained increasing recognition as a potential prognostic and/or diagnostic tool. The objective of this study was to identify ROS-associated biomarkers predictive of survival in patients with sepsis. In-silico analyses of expression profiles allowed the identification of a 21-gene ROS-associated molecular signature that predicts survival in sepsis patients. Importantly, this signature performed well in a validation cohort consisting of sepsis patients aggregated from distinct patient populations recruited from different sites. Our signature outperforms randomly generated signatures of the same signature gene size. Our findings further validate the critical role of ROSs in the pathogenesis of sepsis and provide a novel gene signature that predicts survival in sepsis patients. These results also highlight the utility of peripheral blood molecular signatures as biomarkers for predicting mortality risk in patients with sepsis, which could facilitate the development of personalized therapies.
    Note
    On an institutional repository or open access repository after 12 months embargo.
    ISSN
    2045-8932
    2045-8940
    DOI
    10.1086/685547
    Version
    Final published version
    Sponsors
    Veterans Administration Health System grant [1IK2BX001477]; National Institutes of Health [R01HL91899]
    Additional Links
    http://www.journals.uchicago.edu/doi/10.1086/685547
    ae974a485f413a2113503eed53cd6c53
    10.1086/685547
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